Genetic modifiers in rare disorders: the case of fragile X syndrome

Methods employed in genome-wide association studies are not feasible ways to explore genotype–phenotype associations in rare disorders due to limited statistical power. An alternative approach is to examine relationships among specific single nucleotide polymorphisms (SNPs), selected a priori, and b...

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Detalles Bibliográficos
Autores principales: Crawford, Hayley, Scerif, Gaia, Wilde, Lucy, Beggs, Andrew, Stockton, Joanne, Sandhu, Pria, Shelley, Lauren, Oliver, Chris, McCleery, Joseph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852869/
https://www.ncbi.nlm.nih.gov/pubmed/32862204
http://dx.doi.org/10.1038/s41431-020-00711-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852869/
https://www.ncbi.nlm.nih.gov/pubmed/32862204
http://dx.doi.org/10.1038/s41431-020-00711-x

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